Ghrelin receptor signaling targets segregated clusters of neurons within the nucleus of the solitary tract View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-09

AUTHORS

María Paula Cornejo, Pablo Nicolás De Francesco, Guadalupe García Romero, Enrique L. Portiansky, Jeffrey M. Zigman, Mirta Reynaldo, Mario Perello

ABSTRACT

Ghrelin is a stomach-derived hormone that regulates a variety of biological functions such as food intake, gastrointestinal function and blood glucose metabolism, among others. Ghrelin acts via the growth hormone secretagogue receptor (GHSR), a G-protein-coupled receptor located in key brain areas that mediate specific actions of the hormone. GHSR is highly expressed in the nucleus of the solitary tract (NTS), which is located in the medulla oblongata and controls essential functions, including orofacial, autonomic, neuroendocrine and behavioral responses. Here, we used a mouse model, in which the expression of enhanced green fluorescent protein (eGFP) is controlled by the promoter of GHSR (GHSR-eGFP mice), to gain neuroanatomical and functional insights of the GHSR-expressing neurons of the NTS. We found that GHSR-expressing neurons of the NTS are segregated in clusters that were symmetrically distributed to the midline: (1) a pair of rostral clusters, and (2) a caudal and medially located cluster. We also identified that a subset of GHSR neurons of the caudal NTS are GABAergic. Finally, we found that rostral NTS GHSR neurons increase the levels of the marker of neuronal activation c-Fos in mice exposed to fasting/refeeding or high-fat diet bingeing protocols, while caudal NTS GHSR neurons increase the levels of c-Fos in mice exposed to gastric distension or LiCl-induced malaise protocols. Thus, current data provide evidence that ghrelin receptor signaling seems to target segregated clusters of neurons within the NTS that, in turn, may be activated by different stimuli. More... »

PAGES

3133-3147

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00429-018-1682-5

DOI

http://dx.doi.org/10.1007/s00429-018-1682-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1103992146

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/29761230


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